Research Article | Open Access
Xiaojie Wang, Jianqiang Hao, Gigi Leung, Trisia Breitkopf, Eddy Wang, Nicole Kwong, Noushin Akhoundsadegh, Garth L. Warnock, Jerry Shapiro, Kevin J. McElwee, "Hair Follicle Dermal Sheath Derived Cells Improve Islet Allograft Survival without Systemic Immunosuppression", Journal of Immunology Research, vol. 2015, Article ID 607328, 15 pages, 2015. https://doi.org/10.1155/2015/607328
Hair Follicle Dermal Sheath Derived Cells Improve Islet Allograft Survival without Systemic Immunosuppression
Immunosuppressive drugs successfully prevent rejection of islet allografts in the treatment of type I diabetes. However, the drugs also suppress systemic immunity increasing the risk of opportunistic infection and cancer development in allograft recipients. In this study, we investigated a new treatment for autoimmune diabetes using naturally immune privileged, hair follicle derived, autologous cells to provide localized immune protection of islet allotransplants. Islets from Balb/c mouse donors were cotransplanted with syngeneic hair follicle dermal sheath cup cells (DSCC, group 1) or fibroblasts (FB, group 2) under the kidney capsule of immune-competent, streptozotocin induced, diabetic C57BL/6 recipients. Group 1 allografts survived significantly longer than group 2 (32.2 ± 12.2 versus 14.1 ± 3.3 days, ) without administration of any systemic immunosuppressive agents. DSCC reduced T cell activation in the renal lymph node, prevented graft infiltrates, modulated inflammatory chemokine and cytokine profiles, and preserved better beta cell function in the islet allografts, but no systemic immunosuppression was observed. In summary, DSCC prolong islet allograft survival without systemic immunosuppression by local modulation of alloimmune responses, enhancing of beta cell survival, and promoting of graft revascularization. This novel finding demonstrates the capacity of easily accessible hair follicle cells to be used as local immunosuppression agents in islet transplantation.
Transplantation of pancreatic islets is potentially a curative treatment for type 1 diabetes. However, the systemic immunosuppressive drugs that recipients must use lifelong to prevent rejection of the islet allografts also suppress immunity to other antigens, thereby increasing the risk of opportunistic infections and cancers [1–3]. These drugs also have an adverse impact on the transplanted islets’ survival, causing the function of islets to decline over time, such that many recipients must eventually resume insulin injections for control of blood glucose levels [1–3]. Therefore, a safe and efficient means to protect graft rejection is urgently needed.
Localized immune protection is a feasible means to provide an immune privileged microenvironment to prevent rejection with minimal systemic side effects [4–7]. It has been reported that allogeneic islets could survive in the anterior chamber of the eye ; however, to date, corneal transplantation is the only common clinical procedure that takes advantage of natural immune privilege (IP), due to the feasibility of transplantation from and to the same IP site. Although it seems unlikely that islets could be transplanted into natural IP sites and remain functional in practice, the survival of ectopic IP cells/tissues has led to a novel idea that they could be used in localized, cell-based therapy.
Recent progress using cells with IP properties has explored the potential of cell-based immune modulation as an alternative to immunosuppressive drug therapy in the context of pancreatic islet transplantation [4–8]. Strategies using cells with natural IP properties, such as amniotic epithelial cells or Sertoli cells, derived from the placenta and testis, respectively, have been successfully cotransplanted with isolated islets. Cotransplantation of either amniotic epithelial cells or Sertoli cells sustains islet allograft survival, without systemic immunosuppression, suggesting that a more physiological approach to immune protection of transplanted islets can be achieved. However, the supply of these cells is limited; they are difficult to derive and to maintain in long-term culture.
The hair follicle (HF) constitutes one of the few immunologically privileged tissues besides the brain, eye, placenta, and testis [9–12]. Hair follicle IP has been demonstrated in fully MHC mismatched donor and recipient HF tissue transplantation both in mouse and human studies [10, 13]. New hair was produced in recipients transplanted with the lower parts of HFs from a histoincompatible donor, suggesting that HFs can escape alloimmune attack . Studies into the mechanisms of alopecia areata and lichen planopilaris hair loss reveal that normal hair follicles may avoid autoimmune mediated destruction by downregulating MHC I and II and by upregulating potent immunosuppressive factors [9, 12]. Our group has previously shown that primary HF bulb and cultured dermal sheath cup cells (DSCC) exhibit immune privilege via somatostatin and PD-L1 expression, respectively [13–15].
Hair follicle (HF) cells with IP are readily accessible and they can be derived from HFs of the islet transplant recipient (autologous), suggesting their potential use in personalized immunoprotective transplant medicine. In this study, we examined the effects of cultured DSCC on beta cell survival in a mouse islet transplantation model.
2. Research Design and Methods
2.1. Islet Isolation and Transplantation
C57BL/6 (B6), C3H/HeJ (C3H), and Balb/c mice were purchased from The Jackson Laboratory. All mice were cared for according to the guidelines of the Canadian Council on Animal Care and regulations of the University of British Columbia. Donor islets were isolated by ductal collagenase injection from 8–10-week-old female Balb/c mice . Three groups of 400 islets each were transplanted into the left kidney of 200 mg/kg streptozotocin (Sigma, Oakville, Canada) induced diabetic age-matched recipients one to two weeks prior to transplantation.
400 islets were either mixed with DSCC (group 1) or with dermal fibroblasts (group 2) in a collagen gel , which contained 350 μL 3 × HAM’s F10 medium, 26 μL 0.4 N NaOH, 125 μL FBS, and 870 μL of acid-extracted fetal bovine type-I collagen (5 mg/mL, Sigma), plus DSCC or FB (1 × 105 per graft). Animals were considered as diabetic after two consecutive days with random blood glucose levels >20 mmol/L. Allograft function in transplanted mice was defined as a drop of blood glucose concentration <13.8 mmol/L on day 3 after transplantation, and a graft was considered as rejected when the blood glucose rebounded to a level of >13.8 mmol/L for two consecutive days after normal primary graft success.
2.2. Microdissection of HF Cells
Dermal sheath cup (DSC), dermal papilla (DP), nonbulbar dermal sheath (DS) tissues, and nonfollicular dermal fibroblasts (FB) were isolated from donor mouse vibrissa HFs under a microscope as described [13–15]. The bulb mesenchyme tissue was cut to separate the lowest portion of bulbar dermal sheath cup (DSC) and the DP. The DS is defined as the sheath surrounding the HF that extends from above the bulb region to below the sebaceous gland duct. The individual tissues were cultured in AmnioMax C-100 with supplement (Invitrogen, Burlington, ON).
2.3. Glucose Stimulation Assay
The isolated islets were cultured with DSCC or FB cells in Krebs-Ringer’s Buffer (Sigma) at 37°C for 1 hr after 3 or 7 days of coculture. The supernatant was then replaced with Krebs-Ringer’s Buffer with 2 mmol/L or 20 mmol/L of glucose and cultured for 1 hr and stored for insulin detection. Insulin was measured by ELISA (Crystal Chem., Chicago, IL).
2.4. Mixed-Lymphocyte Reaction Assay (MLR)
The responder splenocytes (SPL) or graft draining renal lymph node (LN) derived cells were isolated from B6 recipients. Responder cells were stimulated with γ-irradiated (2500 rad) Balb/c (allogeneic) or C3H (third party) derived splenocytes at various stimulator/responder ratios for 4 days. BrdU enzyme-linked immunosorbent assay (ELISA; cat#ab126556, Abcam, Toronto, ON, Canada) was performed according to the manufacturer’s instructions. Briefly, the cells were labeled with BrdU for 16 h, followed by fix/denature procedures. The incorporated BrdU was detected at 450 nm after incubation with anti-BrdU peroxidase. IL-2 secretion was detected by using antibody pairs (capture mAb: clone JES6-1A12; detection mAb: clone JES6-5H4) and recombinant protein standard (cat#39-8021) (eBioscience, San Diego, CA).
2.5. Histological Analysis
The transplanted grafts were removed under a microscope and fixed in 4% paraformaldehyde. Paraffin sections (5 μm) were stained with hematoxylin and eosin (H&E). Staining of insulin (DAKO, Burlington, ON, Canada) and CD45 (R&D, Burlington, ON, Canada) was developed using DAB (Sigma).
2.6. Flow Cytometric Analysis
Single-cell suspensions were stained with fluorochrome-conjugated mAbs CD4, CD25, Foxp3, CD69, and CD44 (all eBioscience). Intracellular staining of cytokine IFNγ and IL-2 (eBioscience) was performed after 4 to 5 h phorbol myristate acetate (PMA) plus ionomycin (Sigma) stimulation.
2.7. Quantitative RT-PCR
Total RNA from cultured DSCC, DP, DS, and FB or cultured islets or allografts were extracted by using the RNeasy Mini Kit (Qiagen, Mississauga, Canada) with its on-column RNase-free DNase I procedure. cDNA was then synthesized by Superscript III Reverse Transcriptase (Invitrogen) in 20 μL reaction including 0.5 μg RNA and 150 ng random primer. RNaseH was utilized to remove complementary RNA. QPCR was performed in duplicate using SYBR Green (Applied Biosystems, Carlsbad, CA) in a 10 μL volume containing 1 ng/μL of cDNA and 0.4 μM of each primer (IDT, Toronto, ON, Canada) (Table 1). Relative expression level was expressed as (where CT is cycling threshold) with 18S RNA as the endogenous control for normalization.
2.8. Western Blot
30 to 50 μg of each cell lysate from cultured DSCC or FB () was loaded onto a 12% separating Bis-Tris gel. The proteins were transferred to a nitrocellulose membrane (BioRad, Mississauga, Canada). The membrane was blocked in PBS containing 5% skim milk for 1 h followed by incubation with the primary antibody rabbit anti-mouse BMP6 (ab15640), Inhibin beta A (22689-1-AP), Fgf2 (sc-79, Santa Cruz, Dallas, TX), or mouse anti-actin. The blot was developed with Enhanced Chemiluminescence Plus Developer (Pierce, Nepean, ON, Canada). The protein expression level was calculated using ImageJ software .
2.9. Statistical Analysis
The significance of the Kaplan-Meier survival curve (Figure 2) was determined by log-rank test using Prism software (http://www.prismmodelchecker.org/). The significance of T cell proliferation, expression of T cell subsets, and cytokine production was calculated by two-tailed Student -test or ANOVA. Values are expressed as means ± SEM, and differences are considered significant when .
3.1. DSCC Stimulates Reduced Alloimmune Responses and Promotes Beta Cell Survival In Vitro
We proposed to use cultured HF derived IP cells to protect islet allograft survival. Therefore, we first examined IP-related gene expression in DSCC, DP, and DS cells cultured for 4 passages, relative to FB, by qPCR (Figure 1(a)). Decreased MHC I (H2db), Tap2, and Il1ra and increased Inhba were identified in DSCC at passage 4 compared to FB. Since DSCC differentially expressed more IP-related genes with significance, for example, the lower expression of H2db and Tap2, we compared DSCC to FB in subsequent experiments.
At the protein level, Inhba, which inhibits immune responses [19, 20], was 3.4-fold higher in DSCC compared with FB, suggesting IP might be functionally present in DSCC (Figure 1(a)). In addition, we also found increased expression of bone morphogenetic protein 6 (BMP6), which promotes fetal pancreas development, including insulin-producing beta cells [21, 22], and fibroblast growth factor 2 (Fgf2), which is involved in angiogenesis and is a putative factor involved in islet regeneration [23, 24].
We next evaluated the cells’ ability to promote allogeneic immune responses in a coculture assay. IFNγ was used as a marker for proinflammatory cell activation [14, 15, 25]. A decreased secretion of IFNγ was found in the coculture of splenic leukocytes from Balb/c mice plus DSCC from B6 mice after 5 days of incubation, suggesting the capacity to stimulate allogeneic responses was reduced in DSCC compared with FB (Figure 1(b), versus pg/mL, , ). Furthermore, the percentage of IFNγ+ cells in both CD4+ and CD8+ subsets was also reduced with DSCC coincubation compared with FB (Figure 1(b), CD4+IFNγ+: versus %, ; CD8+IFNγ+: versus %, , ), indicating DSCC reduced both allogeneic CD4+ and CD8+ T cell activation.
This result indicated a potential for DSCC in promoting islet allograft transplantation survival by inhibiting alloreactive T cell activation. We next detected whether DSCC affected islet survival by coculture of DSCC and islets in vitro for 3 or 7 days. An increase of insulin (2.1-fold) and a decrease of Fas (2.8-fold) and Bax (2.2-fold) was detected at the mRNA level in the islets cocultured with DSCC compared with FB, but no statistical significance was found (Figure 1(c)), suggesting some possible beneficial effects of DSCC on islet survival. To further test the effects of DSCC on islet survival, we evaluated beta cell function by static incubation assay. The ability of insulin secretion upon glucose stimulation was significantly improved after 7 days of coculture of isolated islets with DSCC compared with FB (Figure 1(c), versus ng/islet, , ). These results suggested that the ability of DSCC to preserve beta cell function might be through inhibiting apoptotic genes, Fas and Bax, expression.
3.2. DSCC Prolong Islet Graft Survival in a Fully MHC Mismatched Mouse Islet Transplantation Model
Despite the fact that DSCC express IP genes and have the capacity to inhibit T cell proliferation in vitro, there is no direct evidence to show their IP functionality in the context of allogeneic islet transplantation. To investigate the potential local immunosuppressive effect of DSCC, composite grafts of Balb/c derived isolated islets, with DSCC (group 1) or FB (group 2) derived from B6 mice, DSCC only without islets (group 3), and DSCC with islets (group 4, the same as group 1 but nephrectomy was performed 3 weeks after transplant), in a collagen matrix, were transplanted to diabetic immune-competent recipients (B6). Three groups (groups 1, 2, and 4) promptly reversed the blood glucose level of streptozotocin-induced diabetic B6 graft recipients (Figure 2(a)), and group 3 (DSCC only) maintained hyperglycemia, indicating DSCC alone was unable to normalize high glucose levels after transplantation. Mice transplanted with FB and islets (group 2) rejected the allografts around 2 weeks after transplant after establishing primary islet function (Figure 2(a)). In contrast, mice transplanted with DSCC and islets (group 1) showed euglycemia for much longer (Figure 2(b), versus days, , ). During week 2, 6 out of 10 recipients (60%) developed graft failure in group 2, but none of group 1 did (Figure 2(c)). During week 3, the remaining 4 mice in group 2 (40%) all developed hyperglycemia; 2 out of 10 mice in group 1 (20%) also failed. Of mice in group 1, 3 (30%), 1 (10%), 1 (10%), and 3 (30%) developed graft failure during weeks 4, 5, 6, and 7, respectively, indicating a delay in allograft destruction in the presence of DSCC compared with FB (Figure 2(c)). In addition, it was confirmed that the transplanted DSCC and islets were responsible for this prolonged survival since removal of grafts resulted in high glucose (Figure 2(a), group 4).
To further evaluate beta cell function in the transplanted islets, Intraperitoneal glucose tolerance test (IPGTT) was performed on both groups after 2- and 3-week transplantation (Figure 2(d)). Normal responses of islet grafts to IPGTT demonstrated that DSCC-islets were able to function normally in response to glucose stimulation, suggesting maintenance of islet mass.
3.3. DSCC Enhance Angiogenesis
Our observation of delayed allograft rejection and normal response to glucose stimulation in DSCC and islet transplant combinations suggested preservation of beta cell mass. Up to 70% loss of donor islets by isolation and immune rejection in the first week after transplant was found in previous studies [26–28]. Pancreatic islets contain a dense capillary network, approximately 10 times that of surrounding exocrine tissue, for supplying 5 to 10% of the pancreatic blood flow. Similar to islets, HFs also have a high demand for blood supply to ensure hair growth and cycling [27–29]. In fact, HFs have great capacity for stimulating angiogenesis [29–31]. Cotransplantation of islets with HF derived cells that retain their angiogenic properties may be desirable to promote islet vascularization during the early stages of implantation and to help with islet survival. We therefore compared revascularization 1-w posttransplant.
A higher density of infiltrating blood vessels was noticed in the allografts of group 1 (DSCC) mice compared with group 2 (FB, Figure 3(a), versus %, , ) mice. Furthermore, overall size of the blood vessels was bigger in group 1 than in group 2. This was reflected by the numbers of the blood vessels larger than 50 μm in diameter being significantly higher in group 1 compared with group 2 (Figures 3(b) and 3(c), versus %, , ) per field. In addition, the total numbers of the blood vessels were significantly higher in group 1 (Figure 3(d)). The location of the blood vessels is also closer to the transplanted islets in group 1 (Figure 3(b)). In summary, the higher numbers and larger size of the blood vessels in group 1 compared with group 2 demonstrate an enhanced angiogenesis in the presence of DSCC.
3.4. DSCC Modulates Immune Responses in the Draining Lymph Nodes of Transplanted Mice
DSCC stimulated lower alloimmune responses in vitro compared with FB. We next investigated the effects of DSCC on alloimmunity in vivo by examining T cell activation markers CD25, CD69, and CD44 and T cell regulatory marker Foxp3. We observed a significant increase of CD4+Foxp3+ (Figure 4(a), versus %, , ) and CD25+Foxp3+ (Figure 4(b), versus %, , ) and a decrease of CD8+CD69+ (Figure 4(c), versus %, , ) cells in the presence of DSCC compared with FB in the renal lymph nodes of transplanted mice after one week (Figures 4(a) and 4(b)) and two weeks (Figure 4(c)), respectively. However, no significant changes were found at three weeks or in the spleens at any time point (data not shown). These results indicated DSCC did not change the systemic immune profiling in the spleen; instead they locally modulated regulatory T cells (Figures 4(a) and 4(b)) at one week, suggesting the capacity of DSCC to inhibit alloreactive T cell activation partially through upregulating inhibitory T cell subsets. Indeed, reduced T cell activation was detected at two weeks (Figure 4(c)), demonstrating that DSCC also stimulated reduced alloimmune responses in vivo.
3.5. DSCC Prevents Infiltration of Leukocytes into the Allograft
Rejection of transplanted grafts involves destruction of insulin-producing beta cells by leukocytes that infiltrate into the islets. A reduction of graft failure in group 1 (DSCC, Figures 2(a) and 2(b)) may be due to reduced graft inflammatory cell infiltration. Therefore, the development of insulitis, insulin+ cells (beta cell function), and CD45+ cells (infiltrating leukocytes) were examined in group 1 (DSCC) and group 2 (FB) (Figures 5(a)–5(f)). Insulitis was detected in both groups 1 and 2. However, a significantly reduced insulitis was observed in group 1 compared with group 2 at all three time points (Figure 5(d), 1-w, 2-w, and 3-w), suggesting reduced inflammation in the presence of DSCC.
We observed a significant loss of insulin+ cells (more than 50%) 1-w after transplantation in both groups (Figure 5(e), at 1-w versus at 2-w, 53.84% of loss in group 1; at 1-w versus at 2-w, 75.00% of loss in group 2), suggesting severe destruction of transplanted islets by alloreactive leukocytes or other nonimmune factors. However, numbers of insulin+ cells were higher in group 1 compared with group 2 at all three time points, suggesting less damage of beta cells in the presence of DSCC. The better preservation of beta cell function in group 1 may be the result of fewer infiltrating inflammatory (CD45+) cells. Indeed, significantly lower CD45+ cell numbers were found in group 1 compared with group 2 (Figure 5(f), versus at 1-w; versus at 2-w; versus 100 at 3-w, ), suggesting better control of infiltration in the presence of DSCC.
To further investigate the mechanisms of DSCC on islet transplantation, we examined the expression profile of selected chemokines and potent immunosuppressive factors in the transplanted grafts. Quantitative PCR showed a significant decrease of Ccr2 (Th1 chemokine) at 1-w and an increase of Ccr3, Ccr4, Ccr8 (Th2 chemokine), and Il10 (potent immunosuppressive factor) at 3-w in group 1 (DSCC) compared with FB (Figure 5(g)). Thus, promoting a Th2 immune response shift and creating an immunosuppressive microenvironment in the later stages (3-w) by inhibiting Th1 proinflammatory chemokines in early stages (1-w) may be one of the reasons for more limited leukocyte infiltration into DSCC-islet grafts.
3.6. DSCC Protects Transplanted Islets without Systemic Immunosuppression
More limited infiltration of leukocytes (Figure 5) in the allografts from group 1 (DSCC) may result from impaired immunity to alloantigens. To investigate this possibility, MLRs were performed. Results showed similar BrdU incorporation into spleen (SPL) cells in response to either alloantigenic Balb/c or third party control (C3H) splenic leukocytes, suggesting unchanged systemic immune responses in both groups (Figure 6(a)). However, reduced BrdU incorporation was found in the renal lymph node (LN) cells from group 1 (DSCC) mice in response to Balb/c cells but not C3H cells, indicating donor-specific hyporesponsiveness in the local draining lymph nodes (Figure 6(a), 9 : 1 ratio: versus , ; 3 : 1 ratio: versus , , ). This result was confirmed by differences in the total amount of IL-2 secretion (Figure 6(b), versus pg/mL, ). Furthermore, the percentage of IL-2 in both CD4+ and CD8+ subsets in the LN, but not in the SPL in group 1, was lower than that in group 2, demonstrating impaired alloreactive CD4+ and CD8+ T cells in the local LN but not systemically (Figures 6(c), 6(d), and 6(e), CD4+IL-2+: versus , ; CD8+IL-2+: versus , ; ).
Prevention of allograft rejection can be achieved by either systemic or local immunosuppression [1, 16, 17]. Although local immunosuppression controls islet rejection successfully, most studies use gene transfer approaches, which potentially have deleterious effects in human transplantation [16, 17]. Moreover, genetically modified cells typically rely on just one IP conferring product. The use of nongenetically modified cells with natural IP avoids these issues. The concept of controlling alloreactive T cell responses by naturally immune privileged cell therapy has been investigated in several experimental models including islet cell transplantation using amniotic or Sertoli cells [5–8].
In the current study, we showed that cotransplantation of naturally immune privileged HF dermal sheath cup cells (DSCC) with donor islets prolonged allograft survival without systemic antirejection treatments in diabetic immune-competent mice. Consistent with HF IP properties, we showed that cultured DSCC also expressed lower levels of MHC I and related gene Tap2 and a higher level of potent immunosuppressive protein Inhba, compared with non-IP tissue derived FB. The potential of IP status in cultured DSCC was confirmed by both in vitro coculture assay and a fully MHC mismatched mouse islet transplantation model. Several lines of evidence showed that cultured DSCC possessed the capacity to limit alloimmune T cell responses. We first demonstrated DSCC stimulated reduced alloreactive T cell activation using IFNγ as a surrogate maker in an in vitro coculture functional assay. We also showed that DSCC maintained lower CD8+ activation in the local renal draining lymph nodes and attracted a more limited infiltration of leukocytes in MHC mismatched islet allografts.
The transient increase of regulatory T cells in our in vivo model may explain the ability of DSCC to control alloreactive T cell activation. Tregs have been implicated in promoting and maintaining IP status [32–35]. Tregs play a critical role in successful transplantation of corneal tissue which also has IP . Our data provide another line of evidence for the role of Tregs in preserving beta cell function and promoting allograft survival. In addition, a Th1/Th2 shift is also important in determining the outcomes of transplantation and beta cell survival [16, 36]. Our data show that DSCC promote an anti-inflammatory microenvironment in the allograft and shift the Thl/Th2 balance toward Th2.
Our findings suggest significant revascularization of transplants in the presence of DSCC. The rationale behind this finding is closely related to normal HF function. The HF is a mini organ with great regenerative potential since humans are constantly in a state of growing and losing hair. Hair cycling affects blood vessel arrangement around the HF itself and surrounding skin vascularization [29–31]. Encouraging new blood vessel formation could be beneficial for providing essential nutrients and oxygen for beta cell survival since a significant number of donor islets are lost in the early stages after transplant due to poor revascularization and lack of blood supply associated with the isolation and transplantation processes [26–28]. This finding supports the notion of DSCC preserving beta cell mass in multiple ways.
This study for the first time shows that DSCC generate donor-specific tolerance. More importantly, B6 mice implanted with DSCC responded to third party C3H cell stimulation normally, excluding the possibility of nonspecific immune suppression or immune ignorance. Tolerance occurs through various mechanisms including anergy/ignorance and immune regulation/suppression [37–39]. It is well documented that Tregs actively induce tolerance. Our finding of transient upregulation of Tregs suggests their potential involvement in promoting tolerance to the islet grafts. The detailed mechanism underlying this finding is currently under investigation.
Although the idea of using naturally IP DSCC in protection of transplanted islets for treating autoimmune diabetes is promising, more questions need to be answered. For example, different cell numbers and generations can be used for cotransplantation to optimize success rates. Genetic loss or gain of function modification approaches could be employed to examine the relative significance of individual IP conferring factors we have identified in the current study. The finite survival of donor islets in the recipients may appear discouraging at first glance. However, data presented here show that localized, but not systemic, immunosuppression was achieved. Better outcomes may be obtained with more robust, extensive investigations. At a minimum, a DSCC cotransplantation technique could be used with immunosuppressive drug regimens at reduced dose to improve graft survival and eliminate or reduce undesirable side effects.
In conclusion, we demonstrate proof-of-principle in using cultured HF derived cells to create localized immunosuppression without using antirejection drug agents to protect islet allografts as a new potential therapeutic treatment for autoimmune diabetes. DSCC reduce islet allograft rejection through promoting new blood vessel formation and better beta cell survival and limiting alloreactive T cell attack. This result opens new avenues for using cells with natural IP in treating diabetes.
|ELISA:||Enzyme-linked immunosorbent assay|
|MHC I, II:||Major histocompatibility complexes I, II|
|PBMC:||Peripheral blood mononuclear cells|
|qPCR:||Quantitative real-time RT-PCR.|
Conflict of Interests
Kevin J. McElwee is Chief Scientific Officer, and Kevin J. McElwee and Jerry Shapiro are founding shareholders, of Replicel Life Sciences Inc. All other authors declare no conflicts of interest.
Xiaojie Wang researched data, contributed to discussion, wrote the paper, and edited the paper. Jianqiang Hao, Gigi Leung, Nicole Kwong, and Noushin Akhoundsadegh researched data and contributed to discussion. Trisia Breitkopf, Eddy Wang, Garth L. Warnock, and Jerry Shapiro provided new reagents and contributed to discussion. Kevin J. McElwee and Garth L. Warnock contributed to discussion and edited the paper.
This work was supported by grants from the Transplant Research Foundation of British Columbia (TRFBC) Venture Grant program to Garth L. Warnock and Kevin J. McElwee, the Canadian Dermatology Foundation (CDF), and the Canadian Institutes of Health Research (CIHR) to Kevin J. McElwee (NSM-72203). Xiaojie Wang is the recipient of Canadian Institutes of Health Research Skin Research Training Center (CIHR-SRTC) awards and a CIHR postdoctoral fellowship (MFE-123724). Nicole Kwong is a recipient of a Summer Student Research Program (SSRP) Scholarship from the University of British Columbia (UBC). Kevin J. McElwee is a recipient of CIHR (MSH-95328) and Michael Smith Foundation for Health Research (MSFHR, CI-SCH-00480(06-1)) investigator awards. The authors thank Dr. Reza Jalili, Dr. Christopher Carlsten, and Dr. Mandy Pui (University of British Columbia, Vancouver, British Columbia, Canada) for assistance with making collagen gel and FACS acquisition/analysis.
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